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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05149482
Other study ID # 8397
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2021
Est. completion date November 30, 2022

Study information

Verified date November 2021
Source University Hospital, Strasbourg, France
Contact Anne CHARPIOT, MD, PhD
Phone 33 3 88 12 76 41
Email anne.charpiot@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There are only a few cases of isolated lateral canal deficit described in the literature. This study would focus on this group of patients in order to establish an evolving profile, a recovery behavior that we could compare to that in the literature. In addition, the evolving profile as well as the other clinical criteria identified would allow investigators to make hypotheses as to the pathology responsible for a given evolutionary profile. The population studied is represented by adult patients admitted by the emergency consultation service of otolaryngology of the University Hospitals of Strasbourg for an acute unilateral vestibular deficit whose examination at the VHOT shows a reduced and isolated gain of a lateral semicircular canal.


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date November 30, 2022
Est. primary completion date November 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria - Major patient - Man or woman - Patient who has given their consent to the use of their data. - Patient treated in the ENT department for dizziness between June 2020 and July 2021. Non-inclusion criteria - Patient who expressed his opposition to participating in the study - Inability to provide the subject with enlightened information (difficulties in understanding the subject, cognitive disorders) - Subject under safeguard of justice - Subject under guardianship or guardianship - Neurological signs on clinical examination

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Oto-rhino-laryngologie et Chirurgie cervico-faciale - Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Establish the evolutionary profiles of patients with isolated lateral canal involvement 1 month
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